Disease Browser
Parent Node: Lens Diseases (D007905) ..Starting node Cataract (D002386) Child Nodes:
........Absent corpus callosum cataract immunodeficiency (C535566) ........Adams Nance syndrome (C538224) ........Adult i Blood Group with Congenital Cataract (C566214) ........Alpha-B Crystallinopathy (C563848) ........Alpha-B Crystallinopathy with Cataract (C563849) ........Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract (C566280) ........Anterior polar cataract 2 (C537774) ........Arachnodactyly ataxia cataract aminoaciduria mental retardation (C537424) ........Ataxia-Microcephaly-Cataract Syndrome (C563086) ........Autosomal recessive nonsyndromic congenital nuclear cataract (C537298) ........Bassoe syndrome (C537661) ........Bhaskar Jagannathan syndrome (C535437) ........CAHMR syndrome (C537959) ........CAMFAK syndrome (C537965) ........Capsule Opacification (D058442) ........CATARACT 23 (OMIM:610425) ........CATARACT 3, MULTIPLE TYPES (OMIM:601547) ........CATARACT 32, MULTIPLE TYPES (OMIM:115650) ........CATARACT 4, MULTIPLE TYPES (OMIM:115700) ........CATARACT 6, MULTIPLE TYPES (OMIM:116600) ........Cataract and cardiomyopathy (C538280) ........Cataract and congenital ichthyosis (C538281) ........Cataract anterior polar dominant (C538282) ........Cataract ataxia deafness (C538283) ........Cataract congenital dominant non nuclear (C538284) ........Cataract congenital Volkmann type (C538285) ........Cataract Hutterite type (C538286) ........Cataract microcornea syndrome (C538287) ........Cataract, Age-Related Cortical, 1 (C563812) ........Cataract, Age-Related Cortical, 2 (C567814) ........Cataract, Age-Related Nuclear (C563333) ........Cataract, alopecia, sclerodactyly (C535336) ........Cataract, Autosomal Dominant (C565815) ........Cataract, Autosomal Dominant Nuclear (C565137) ........Cataract, Autosomal Dominant, Multiple Types 1 (C566909) ........Cataract, Autosomal Recessive Congenital 1 (C565136) ........Cataract, autosomal recessive congenital 2 (C535337) ........Cataract, Autosomal Recessive Congenital 3 (C567835) ........Cataract, Autosomal Recessive, Early-Onset, Pulverulent (C565298) ........Cataract, Central Saccular, With Sutural Opacities (C565301) ........Cataract, Congenital Nuclear, Autosomal Recessive 1 (C563728) ........Cataract, Congenital Nuclear, Autosomal Recessive 2 (C565725) ........Cataract, Congenital Nuclear, Autosomal Recessive 3 (C566923) ........CATARACT, CONGENITAL OR JUVENILE (OMIM:212500) ........Cataract, Congenital Zonular, with Sutural Opacities (C563435) ........Cataract, Congenital, Cerulean Type, 2 (C563294) ........Cataract, Congenital, Cerulean Type, 3 (C563819) ........Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy (C564353) ........Cataract, congenital, with microcornea or slight microphthalmia (C535338) ........Cataract, Coppock-Like (C565133) ........Cataract, Cortical Pulverulent, Late-Onset (C563604) ........Cataract, Cortical, Juvenile-Onset (C566955) ........Cataract, Crystalline Aculeiform (C566162) ........Cataract, Crystalline Coralliform (C566161) ........Cataract, Floriform (C566160) ........Cataract, Juvenile, With Microcornea And Glucosuria (C567434) ........Cataract, Lamellar 2 (C566481) ........Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome (C566861) ........Cataract, Nuclear Diffuse Nonprogressive (C566157) ........Cataract, Nuclear Progressive (C564596) ........Cataract, Nuclear Total (C566156) ........Cataract, Polymorphic and Lamellar (C563603) ........Cataract, posterior polar, 1 (C535339) ........Cataract, Posterior Polar, 2 (C565134) ........Cataract, posterior polar, 3 (C535343) ........Cataract, posterior polar, 4 (C535344) ........Cataract, posterior polar, 5 (C535340) ........Cataract, Progressive Polymorphic Cortical (C565130) ........Cataract, Pulverulent (C563426) ........Cataract, Pulverulent, Juvenile-Onset (C565703) ........Cataract, Punctate, Progressive Juvenile-Onset (C565131) ........Cataract, Sutural, with Punctate and Cerulean Opacities (C564619) ........Cataract, Variable Zonular Pulverulent (C565132) ........Cataract, zonular (C535342) ........Cataract, Zonular Central Nuclear (C565135) ........Cataract, Zonular Pulverulent 1 (C566158) ........Cataract, Zonular Pulverulent 3 (C566608) ........Cataracts, ataxia, short stature, and mental retardation (C535345) ........Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation (C563390) ........Cerebrooculofacioskeletal Syndrome 2 (C565185) ........Cerebrooculofacioskeletal Syndrome 4 (C565184) ........Cerulean cataract (C537955) ........Cochleosaccular degeneration of the inner ear and progressive cataracts (C536432) ........Congenital Cataracts, Facial Dysmorphism, And Neuropathy (C565822) ........Cornea guttata with anterior polar cataract (C535471) ........Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271) ........Crome syndrome (C536216) ........Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly (C563840) ........Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467) ........Dementia, familial Danish (C538209) ........Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408) ........Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis (C563430) ........Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts (C565596) ........Fine-Lubinsky syndrome (C537933) ........Flynn Aird syndrome (C537066) ........Goldstein Hutt syndrome (C537282) ........Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264) ........HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730) ........Hydrocephalus, endocardial fibroelastosis, and cataracts (C535855) ........Hyperferritinemia, hereditary, with congenital cataracts (C538137) ........Hypertrophic Neuropathy And Cataract (C565490) ........Kahrizi Syndrome (C567196) ........Karandikar Maria Kamble syndrome (C537009) ........Kozlowski Rafinski Klicharska syndrome (C537509) ........Krasnow Qazi syndrome (C537616) ........Leg, Absence Deformity of, with Congenital Cataract (C565442) ........Leukodystrophy, Hypomyelinating, 5 (C567166) ........Lipodystrophy with Congenital Cataracts and Neurodegeneration (C564669) ........Lubinsky syndrome (C543092) ........Marinesco-Sjogren-like syndrome (MSLS) (C535913) ........Marshall syndrome (C536025) ........Martsolf syndrome (C536028) ........Microcephalic primordial dwarfism Toriello type (C537321) ........Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849) ........Microcephaly, Retinitis Pigmentosa, and Sutural Cataract (C563296) ........Microphthalmia, Cataracts, and Iris Abnormalities (C566448) ........Microphthalmia, Isolated, with Cataract 1 (C563582) ........Microphthalmia, Isolated, with Cataract 2 (C565876) ........Microphthalmia, Isolated, with Cataract 3 (C564452) ........Microphthalmia, Isolated, with Cataract 4 (C566480) ........Microphthalmia, syndromic 2 (C537465) ........Mousa Al din Al Nassar syndrome (C536989) ........Muscular dystrophy, congenital, infantile with cataract and hypogonadism (C537385) ........Myopathy, Cataract, Hypogonadism Syndrome (C563578) ........Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769) ........Nance-Horan syndrome (C538336) ........Nathalie syndrome (C538342) ........O'Donnell Pappas syndrome (C537858) ........Optic atrophy and cataract, autosomal dominant (C537128) ........Osteogenesis imperfecta congenita, microcephaly, and cataracts (C537558) ........Pavone Fiumara Rizzo syndrome (C536313) ........Peters anomaly with cataract (C537885) ........Polycystic Kidney, Cataract, and Congenital Blindness (C564882) ........Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203) ........Premature aging, Okamoto type (C535270) ........Schaap Taylor Baraitser syndrome (C536626) ........Seemanova Lesny syndrome (C537536) ........Seow Najjar syndrome (C537584) ........Singh Chhaparwal Dhanda syndrome (C537341) ........Slavotinek Pike Mills Hurst syndrome (C536672) ........Spastic paraplegia 9, autosomal dominant (C536868) ........Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515) ........Spondyloocular Syndrome, Autosomal Recessive (C565285) ........Warburg Sjo Fledelius syndrome (C536681) ........Wellesley Carmen French syndrome (C536691) ........Zonular cataract and nystagmus (C536727) Sister Nodes: ..Aphakia (D001035) ..Artificial Lens Implant Migration (D060437) ..Cataract (D002386) ..Lens Subluxation (D007906) UMLS . MedGen , OMIM , CTD
Cataract 
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